herissm art tot mengaib yarana bosat sit wend (d Treating allylbenzene with aqueous H₂SO4 causes it to rearrange to B-methylstyrene as shown below. Use curved arrow formalism to draw a mechanism for this process. allylbenzene B-methylstyrene

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**Rearrangement of Allylbenzene to β-Methylstyrene**

In this process, treating allylbenzene with aqueous H2SO4 causes it to rearrange to β-methylstyrene. The structural transformation is illustrated below:

### Chemical Structures
1. **Allylbenzene**:
   - Structure: Shows a benzene ring bonded to a three-carbon chain with a double bond (allyl group).

2. **Rearrangement Process**:
   - An arrow indicates the transformation from allylbenzene to β-methylstyrene.

3. **β-Methylstyrene**:
   - Structure: Displays a benzene ring connected to a two-carbon chain with a double bond and a methyl group.

### Mechanism
- Use curved arrow formalism to draw a reasonable mechanism for this process. The curved arrow indicates the movement of electrons during the transformation, leading to the rearrangement of the double bond position resulting in β-methylstyrene.

For educational purposes, understanding the electron movement and structural changes during this reaction is critical to predict patterns in chemical reactivity and syntheses.
Transcribed Image Text:**Rearrangement of Allylbenzene to β-Methylstyrene** In this process, treating allylbenzene with aqueous H2SO4 causes it to rearrange to β-methylstyrene. The structural transformation is illustrated below: ### Chemical Structures 1. **Allylbenzene**: - Structure: Shows a benzene ring bonded to a three-carbon chain with a double bond (allyl group). 2. **Rearrangement Process**: - An arrow indicates the transformation from allylbenzene to β-methylstyrene. 3. **β-Methylstyrene**: - Structure: Displays a benzene ring connected to a two-carbon chain with a double bond and a methyl group. ### Mechanism - Use curved arrow formalism to draw a reasonable mechanism for this process. The curved arrow indicates the movement of electrons during the transformation, leading to the rearrangement of the double bond position resulting in β-methylstyrene. For educational purposes, understanding the electron movement and structural changes during this reaction is critical to predict patterns in chemical reactivity and syntheses.
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